Canonical Allele Identifier: CA514475139

Gene: CACNG2

Linked Data

• MyVariant Identifiers: chr22:g.36960695G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36564648G>C , CM000684.2:g.36564648G>C	GRCh38
NC_000022.10:g.36960695G>C , CM000684.1:g.36960695G>C	GRCh37
NC_000022.9:g.35290641G>C	NCBI36
NG_031861.1:g.142996C>G
NG_031861.2:g.143211C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300105.7:c.675C>G MANE Select	ENSP00000300105.6:p.Arg225=
ENST00000300105.6:c.675C>G	ENSP00000300105.6:p.Arg225=
NM_006078.3:c.675C>G	NP_006069.1:p.Arg225=
NM_006078.4:c.675C>G	NP_006069.1:p.Arg225=
XM_017028531.2:c.417C>G	XP_016884020.1:p.Arg139=
NM_001379051.1:c.606C>G	NP_001365980.1:p.Arg202=
NM_006078.5:c.675C>G MANE Select	NP_006069.1:p.Arg225=
NR_166440.1:n.2041C>G